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Effects of Geometric Isomerism and Anions on the Kinetics and Mechanism of the Stepwise Formation of Long-Range DNA Interstrand Cross-Links by Dinuclear Platinum Antitumor Complexes

机译:几何异构和阴离子对双核铂抗肿瘤复合物逐步形成远距离DNA链间交联的动力学和机理的影响

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摘要

Reported herein is a detailed study of the kinetics and mechanism of formation of a 1,4-GG interstrand cross-link by the dinuclear platinum anticancer compound [15N][{cis-PtCl(NH3)2}2{孎H2(CH2)6NH2}]2+ (1,1/c,c (1)). The reaction of [15N]1 with 5'-{d(ATATGTACATAT)2} (I) has been studied by [1H,15N] HSQC NMR spectroscopy in the presence of different concentrations of phosphate. In contrast with the geometric trans isomer (1,1/t,t), there was no evidence for an electrostatic preassociation of 1,1/c,c with the polyanionic DNA surface, and the pseudo-first-order rate constant for the aquation of [15N]1 was actually slightly higher (rather than lower) than that in the absence of DNA. When phosphate is absent, the overall rate of formation of the cross-link is quite similar for the two geometric isomers, occurring slightly faster for 1,1/t,t. A major difference in the DNA binding pathways is the observation of phosphate-bound intermediates only in the case of 1,1/c,c. 15 mM phosphate causes a dramatic slowing in the overall rate of formation of DNA interstrand cross-links due to both the slow formation and slow closure of the phosphate-bound monofunctional adduct. A comparison of the molecular models of the bifunctional adducts of the two isomers shows that helical distortion is minimal and globally the structures of the 1,4 interstrand cross-links are quite similar. The effect of carrier ligand was investigated by similar studies of the ethylenediamine derivative [15N]1-en. A pKa value of 5.43 was determined for the [15N]1,1/c,c-en diaquated species. The rate of reaction of [15N]1-en with duplex I is similar to that of 1,1/c,c and the overall conformation of the final adduct appears to be similar. The significance of these results to the development of "second-generation" polynuclear platinum clinical candidates based on the 1,1/c,c chelate (dach) series is discussed.
机译:本文报道了双核铂抗癌化合物[15N] [{顺式-PtCl(NH3)2} 2 {= H2(CH2)]形成1,4-GG链间交联的动力学和机理的详细研究。 6NH2}] 2+(1,1 / c,c(1))。 [15N] 1与5'-{d(ATATGTACATAT)2}(I)的反应已通过[1H,15N] HSQC NMR光谱在不同浓度的磷酸盐存在下进行了研究。与几何反式异构体(1,1 / t,t)相比,没有证据表明1,1 / c,c与聚阴离子DNA表面发生静电预缔合,并且没有假的一级速率常数。实际上,[15N] 1的水合比没有DNA的水合稍高(而不是低)。当不存在磷酸盐时,两种几何异构体的交联形成的总速率非常相似,在1,1 / t,t时发生的速度略快。 DNA结合途径的主要区别是仅在1,1 / c,c情况下观察到磷酸盐结合的中间体。由于磷酸盐结合的单官能加合物的缓慢形成和缓慢闭合,15 mM磷酸盐导致DNA链间交联的整体形成速率急剧降低。两种异构体的双官能加合物的分子模型比较表明,螺旋形变形最小,并且整体上,1,4链间交联的结构非常相似。通过对乙二胺衍生物[15N] 1-en的类似研究研究了载体配体的作用。对于[15N] 1,1 / c,c-en渗入物种,pKa值为5.43。 [15N] 1-en与双链体I的反应速率与1,1 / c,c相似,最终加合物的总体构象似乎相似。讨论了这些结果对基于1,1 / c,c螯合物(dach)系列的“第二代”多核铂临床候选药物开发的意义。

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